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FDA Grants Orphan Drug Designation for Investigational WT1 Cancer Peptide Vaccine DSP-7888 americanpharmaceuticalreview
July 11, 2017
Boston Biomedical announced the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) for DSP-7888, an investigational cancer peptide vaccine, for the treatment of myelodysplastic syndrome (MDS).
FDA approves Bristol-Myers Squibb’s Orencia for active psoriatic arthritis pharmaceutical-technology
July 11, 2017
The US Food and Drug Administration (FDA) has approved Bristol-Myers Squibb’s Orencia for the treatment of adult patients with active psoriatic arthritis (PsA).
Novartis combination targeted therapy receives FDA approval europeanpharmaceuticalreview
July 10, 2017
The FDA has approved Novartis’ Tafinlar (dabrafenib) in combination with Mekinist (trametinib) to treat patients with metastatic non-small cell lung cancer.
NDA of FDA in 2017 Q2: Total Number of New Drugs Approved Having Surpassed That of the 2016 en-cphi.cn
July 07, 2017
With a half of 2017 past, unlike the downturn experienced in 2016, the new drug approval of FDA in 2017 can be called sailing with the wind...
EMA and FDA harmonise over development of Gaucher drugs pharmafile
July 06, 2017
The EMA and the FDA have announced that they have developed a joint proposal to promote more efficient means of bringing through treatments for Gaucher disease.
EMA and FDA aim to slash Gaucher disease R&D costs pharmaphorum
July 06, 2017
US and European regulators want to promote the development of drugs for paediatric Gaucher disease, moves which could also apply to other rare diseases in children.
EMA and FDA propose new approach for Gaucher disease drug development pharmaceutical-technology
July 06, 2017
The European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) have proposed new approaches to the development of medicine to treat Gaucher disease.
FDA announces a strategic plan to eliminate orphan designation backlog biospectrumasia
July 05, 2017
The agency intends to communicate around the successful elimination of the backlog by mid-September.
Wockhardt receives US FDA approval for Olopatadine HCI financialexpress
July 04, 2017
Olopatadine HCI, eye drop to treat ophthalmic allergies, is a generic version of Patanol
FDA approves Vectibix for use in wild-type RAS metastatic colorectal cancer cphi-online
July 04, 2017
First-and-only fully human monoclonal anti-epidermal growth factor receptor antibody approved by the FDA for this patient population.

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